Canonical Allele Identifier: CA1104138181

Gene: ABCB1

Linked Data

• dbSNP Id: rs1817616409
• gnomAD v3: 7-87562780-A-AC
• gnomAD v4: 7-87562780-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87562780_87562781insC , CM000669.2:g.87562780_87562781insC	GRCh38
NC_000007.13:g.87192096_87192097insC , CM000669.1:g.87192096_87192097insC	GRCh37
NC_000007.12:g.87030032_87030033insC	NCBI36
NG_011513.1:g.155468_155469insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.703-1394_703-1393insG	ENSP00000265724.3:n.703-1394_703-1393insG
ENST00000622132.5:c.703-1394_703-1393insG MANE Select	ENSP00000478255.1:n.703-1394_703-1393insG
ENST00000265724.7:c.703-1394_703-1393insG	ENSP00000265724.3:n.703-1394_703-1393insG
ENST00000543898.5:c.511-1394_511-1393insG	ENSP00000444095.1:n.511-1394_511-1393insG
ENST00000622132.4:c.703-1394_703-1393insG	ENSP00000478255.1:n.703-1394_703-1393insG
NM_000927.4:c.703-1394_703-1393insG	NP_000918.2:n.703-1394_703-1393insG
NM_001348944.1:c.703-1394_703-1393insG	NP_001335873.1:n.703-1394_703-1393insG
NM_001348945.1:c.913-1394_913-1393insG	NP_001335874.1:n.913-1394_913-1393insG
NM_001348946.1:c.703-1394_703-1393insG	NP_001335875.1:n.703-1394_703-1393insG
NM_001348946.2:c.703-1394_703-1393insG MANE Select	NP_001335875.1:n.703-1394_703-1393insG
NM_000927.5:c.703-1394_703-1393insG	NP_000918.2:n.703-1394_703-1393insG
NM_001348944.2:c.703-1394_703-1393insG	NP_001335873.1:n.703-1394_703-1393insG
NM_001348945.2:c.913-1394_913-1393insG	NP_001335874.1:n.913-1394_913-1393insG